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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02568137
Other study ID # R21NS094033
Secondary ID
Status Completed
Phase N/A
First received July 13, 2015
Last updated September 29, 2017
Start date January 2017
Est. completion date July 2017

Study information

Verified date April 2017
Source Medical University of South Carolina
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research seeks to develop a culturally-acceptable, effective, and sustainable way of utilizing the rapidly growing penetration of mobile phones among people in Sub-Saharan Africa (SSA), to improve the currently poor control of hypertension among patients at high risk for future stroke. It also aims to develop human capital in SSA to conduct locally-relevant, high-quality stroke research in the future. Specifically, this study will preliminarily test a strategy that incorporates mobile phone texting and home blood pressure monitoring directed by trained nurses, to improve patient adherence to proven medical therapies for treating hypertension.


Description:

Uncoordinated care and shortage of physicians limit the capacity of countries in Sub-Saharan Africa (SSA) to implement effective and sustainable control of hypertension in routine clinical practice. Of the various cardiovascular disease entities, none is more strongly linked to hypertension than stroke. Recent estimates indicate that death from stroke in low-income and middle-income countries (LMIC) account for roughly 4 out of 5 stroke-related deaths worldwide, and the disability adjusted life years lost in these countries is almost seven times those lost in high-income countries (HIC). Most of these LIMC are in SSA. Moreover, given the transition from primarily infectious conditions to chronic non-communicable diseases, the burden of stroke in SSA is likely to increase substantially over the next several decades. Fortunately, with proper control of hypertension, the incidence of and mortality from stroke can be greatly reduced, as has been recently witnessed in several HIC. Despite its immense burden of stroke, SSA has the lowest density of neurologists worldwide, a situation exacerbated by the migration of providers and researchers to industrialized countries. Thus, an urgent priority in SSA is to develop human capital in the region to investigate and enhance stroke outcomes by partnering with established researchers. The theoretically-based Phone-based Intervention under Nurse Guidance after Stroke (PINGS) intervention will comprise protocol-driven mHealth technology (remote home blood pressure monitoring and mobile phone texting) under the guidance of nurse navigators, among patients with hypertension who have experienced a recent stroke (within one month of symptom onset) in Kumasi, Ghana. In Phase 1, the investigators will conduct a 3-month feasibility randomized trial with 6-month follow-up among 60 stroke patients with uncontrolled hypertension, randomly assigned to standard care or PINGS. The investigators will assess key methodological parameters, consumer responses, and clinical outcomes including recruitment and retention rates, intervention use, patient/provider satisfaction, real time medication adherence rates, medication possession ratios, and post-discharge clinic blood pressure levels. In Phase 2, the investigators will triangulate data from Phase 1 to further refine and optimize PINGS and prepare for a full-scale future efficacy/ effectiveness randomized clinical trial. Throughout PINGS, researchers in the United States will mentor their co-investigators in Ghana and impart knowledge about developing mHealth research capacity. Successful completion of PINGS will lead to a cadre of investigators in Ghana knowledgeable about clinical research methodology, and experienced in the execution of innovative, contextualized research targeted at stroke.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Above the age of 18 years; male or female

2. Index stroke symptoms began no greater than one month before enrollment

3. Uncontrolled hypertension (SBP =140 mmHg) based upon last inpatient or outpatient encounter clinic within previous 12 months

4. Legally competent

5. Owns or has close home-sharing family member with a cell phone

Exclusion Criteria:

1. Failure to meet any inclusion criteria

2. Severe cognitive impairment/dementia (Modified Mini-Mental Score [MMSE] =24)*

3. Severe global disability (modified Rankin Scale Score [mRS] = 3)*

4. Renal dialysis; awaiting renal transplant or transplant recipient

5. Cancer diagnosis or treatment in past 2 years

6. Planned pregnancy

7. Vulnerable populations such as pregnant or nursing women, prisoners, and institutionalized individuals.

- MMSE =24 and global disability (mRS = 3) excludes patients who have severe cognitive impairments and medical limitations that would interfere with adequate participation in the PINGS project.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Smart-phone based technology


Locations

Country Name City State
Ghana Kwame Nkrumah University of Science and Technology Kumasi

Sponsors (2)

Lead Sponsor Collaborator
Medical University of South Carolina Kwame Nkrumah University of Science and Technology

Country where clinical trial is conducted

Ghana, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recruitment rates 9 months
Primary Patient Satisfaction Scales 9 months
Primary Clinic based Blood Pressure 9 months
Primary Retention rates 9 months
Secondary Med Possession Ratio 9 months
Secondary Morisky Med Adherence Scale 9 months
Secondary Provider Satisfaction Scales 9 months
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